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Michael-Titus, A. T.

Publications and source records attributed to Michael-Titus, A. T..

2 recordsLinked to original sources

Brief, repeated isoflurane anaesthesia elicits sex-dependent behavioural, cerebrovascular, and microglial alterations in mice

General anaesthetics are indispensable tools in biomedical research, yet growing evidence shows that their effects on brain function extend beyond the transient loss of consciousness for which they are used. Although numerous preclinical studies have examined the impact of a single anaesthetic exposure, far less is known about the cumulative consequences of repeated administration protocols, despite their widespread use in longitudinal imaging, behavioural testing, and disease model studies. Here, we show that brief, repeated isoflurane exposures induce alterations in behaviour, cerebrovascular patterns, and microglial phenotype in adult CD1 mice, with several responses exhibiting pronounced sex specificity. Repeated anaesthesia suppressed locomotor activity selectively in females and impaired ethologically important maintenance behaviours, including nesting and burrowing, in both sexes. These behavioural effects were accompanied by sex-dependent changes in cerebral blood flow dynamics, with females displaying elevated cerebrovascular flow, yet males showing higher reactivity to isoflurane exposure. At the molecular level, repeated isoflurane exposure altered endothelial marker expression without modifying capillary density and shifted microglia toward a hyporeactive state. Together, these data reveal that even short, routine anaesthetic events produce biologically meaningful and sex-dependent effects on neural, vascular, and immune systems. These results indicate that the anaesthetic regimen is an often overlooked but influential factor that deserves careful consideration in pre-clinical neuroscience.

neuroscience↗

Plasma membrane transporter Progressive Ankylosis Protein Homolog (ANKH/Ankh) mediates senescence-derived extracellular citrate and is regulated by DNA damage, inflammation and ageing

A considerable body of recent evidence supports citrate transport as a major regulator of organismal lifespan and healthspan. Citrate accumulates outside senescent cells in vitro and in vivo. However, the detailed mechanism of senescent cell extracellular citrate (EC) accumulation is not clear. We show here that EC is partially mediated by a newly described plasma membrane citrate transporter ANKH/SLC62A1 (progressive human ankylosis - ANKH) in senescent fibroblasts. Analogous to interleukin 6 (IL-6), EC and/or ANKH are regulated by telomere dysfunction, the p38 mitogen-activated kinase axis, transforming growth factor beta and p53, but in contrast not by steroids, sodium butyrate, or Ataxia Telangiectasia Mutated (ATM). ANKH was upregulated in other senescent cell types relevant to ageing but not keratinocytes. In contrast, EC and ANKH were inhibited in dividing and senescent fibroblasts by interleukin 1 (IL-1) in parallel with increased IL-6 secretion. Loss- and gain of function mutations of ANKH/Ank are associated with disease and interestingly, Ank is also downregulated in both aged mouse liver and brain tissues in parallel with increased senescence markers and several cytokines, suggesting that inflammatory cytokines could inhibit EC production in vivo. These data identify ANKH/Ank as a novel regulator of senescence-derived EC in both humans and mice. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=82 SRC="FIGDIR/small/609895v3_ufig1.gif" ALT="Figure 1"> View larger version (21K): org.highwire.dtl.DTLVardef@1eed642org.highwire.dtl.DTLVardef@1349040org.highwire.dtl.DTLVardef@1ea867aorg.highwire.dtl.DTLVardef@22d251_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗